Temporal artery involvement in AL amyloidosis: an important differential diagnosis for giant cell arteritis. A case report and literature review

2019 ◽  
Vol 4 (1) ◽  
pp. 90-94
Author(s):  
Hiroshi Oiwa ◽  
Nagaaki Katoh ◽  
Shoichiro Kojo ◽  
Tsuneaki Yoshinaga ◽  
Kohei Taniguchi ◽  
...  

2019 ◽  
Vol 2019 ◽  
pp. 1-3
Author(s):  
Philipp Arens ◽  
Andrea Ullrich ◽  
Heidi Olze ◽  
Florian Cornelius Uecker

An osseous choristoma is a benign tumor consisting of regular bone tissue in an irregular localization. Choristomas in the head and neck region are rare. Most frequently, they are found in the region of the tongue or oral mucosa. There are also very few reports on osseous choristomas in the submandibular region. We present the case of a woman with a large, caudal osseous choristoma within the lateral cervical triangle. Literature review is given about all of the reported cases in the region of the neck. The pathogenesis is yet unexplained. Our case supports the theory that the development of an osseous choristoma is a reaction to a former trauma. Cervical osseous choristomas are seldom, but they represent an important differential diagnosis when dealing with a cervical tumor.



Rheumatology ◽  
2019 ◽  
Vol 58 (Supplement_2) ◽  
Author(s):  
Emma Rubenstein ◽  
Carla Maldini ◽  
Solange Gonzalez-Chiappe ◽  
Sylvie Chevret ◽  
Alfred Mahr


2017 ◽  
Vol 2017 ◽  
pp. 1-5 ◽  
Author(s):  
Rafael Alex Barbosa de Siqueira Sobrinho ◽  
Karolina Cayres Alvino de Lima ◽  
Helena Carvalho Moura ◽  
Mônica Modesto Araújo ◽  
Christyanne Maria Rodrigues Barreto de Assis ◽  
...  

Giant cell arteritis is a form of vasculitis involving the medium- and large-sized arteries that chiefly affects older people. Clinical findings are headache, jaw claudication, fever, pain, and thickening of the temporal artery. The most feared complication is visual loss due to impairment of the ophthalmic artery and posterior ciliary arteries. This a case report of an 85-year-old male presenting with headache and jaw pain, who was admitted with tongue necrosis as an initial manifestation of giant cell arteritis. The necrotic area detached spontaneously after two weeks of therapy with corticosteroids and methotrexate. Reviewing the literature, our patient presented with clinical symptoms consistent with most reports, except for the fact of being male. Although unusual as an initial manifestation, tongue necrosis is an important alert for diagnosing giant cell arteritis. Early diagnosis and treatment of this atypical manifestation may reduce morbidity.



1987 ◽  
Vol 18 (11) ◽  
pp. 1186-1189 ◽  
Author(s):  
Philip B. Clement ◽  
Harry Senges ◽  
Angela R. How




2007 ◽  
Vol 23 (4) ◽  
pp. 195-198 ◽  
Author(s):  
Long-Wei Lin ◽  
Shoei-Shen Wang ◽  
Chia-Tung Shun


Cureus ◽  
2020 ◽  
Author(s):  
Francisco J Cuevas Castillo ◽  
Sunam Sujanani ◽  
Vishaka K Chetram ◽  
Mohanad Elfishawi ◽  
Adriana Abrudescu


Sign in / Sign up

Export Citation Format

Share Document